Supporting Information
Supporting information features procedures for synthesis of chiral α-linoleoyl glycerols, physicochemical properties of synthetic compounds, HRESITOF mass spectrometric analysis of nostochopcerol (1), copies of NMR spectra for 1, 3-linoleoyl-1,2-O-isopropylidene-sn-glycerol (2b), and 1-linoleoyl-sn-glycerol (3a).
| Supporting Information File 1: Experimental details, characterization data and copies of spectra. | ||
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Cite the Following Article
Nostochopcerol, a new antibacterial monoacylglycerol from the edible cyanobacterium Nostochopsis lobatus
Naoya Oku, Saki Hayashi, Yuji Yamaguchi, Hiroyuki Takenaka and Yasuhiro Igarashi
Beilstein J. Org. Chem. 2023, 19, 133–138.
https://doi.org/10.3762/bjoc.19.13
How to Cite
Oku, N.; Hayashi, S.; Yamaguchi, Y.; Takenaka, H.; Igarashi, Y. Beilstein J. Org. Chem. 2023, 19, 133–138. doi:10.3762/bjoc.19.13
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Scholarly Works
- Weiss, M. B.; Borges, R. M.; Sullivan, P.; Domingues, J. P. B.; da Silva, F. H. S.; Trindade, V. G. S.; Luo, S.; Orjala, J.; Crnkovic, C. M. Chemical diversity of cyanobacterial natural products. Natural product reports 2024. doi:10.1039/d4np00040d
